Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 914643-08-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 3-amino-2-chloro-4-methylbenzoate features a trifunctional aromatic core with amino, chloro, and ester groups positioned for orthogonal reactivity. The electron-donating amino moiety enhances nucleophilicity at the meta site, while the ortho-chloro substituent enables selective cross-coupling. This bench-stable derivative supports streamlined synthesis of bioactive intermediates in medicinal chemistry.
Methyl 3-amino-2-chloro-4-methylbenzoate serves as a versatile intermediate in medicinal chemistry, enabling the construction of substituted benzimidazoles and other heterocyclic scaffolds. Its amino and chloro groups offer orthogonal reactivity for sequential functionalization, while the methyl ester facilitates downstream derivatization. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling and cyclization protocols common to API development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: